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Small Molecules Targeting H3K9 Methylation Prevent Silencing of Reactivated FMR1 Alleles in Fragile X Syndrome Patient Derived Cells

In fragile X syndrome (FXS), expansion of a CGG repeat tract in the 5′-untranslated region of the FMR1 gene to >200 repeats causes transcriptional silencing by inducing heterochromatin formation. Understanding the mechanism of FMR1 silencing is important as gene reactivation is a potential treatm...

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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Kumari, Daman, Sciascia, Nicholas, Usdin, Karen
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7230530/
https://ncbi.nlm.nih.gov/pubmed/32230785
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11040356
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